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shanshan2010: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú 2013-12-11 10:44:09
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shanshan2010: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú 2013-12-11 10:44:09
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²éѯ½á¹û£º¹²²éµ½150¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . anhydrocinnzeylanine C22H32O7 ÏàËÆ¶È:71.4% Chemical & Pharmaceutical Bulletin 1980 28 1432-1436 The Constituents of Cinnamomi Cortex. I. Structures of Cinncassiol A and Its Glucoside AKIRA YAGI,NOBUTAKA TOKUBUCHI,TOSHIHIRO NOHARA,GENICHIRO NONAKA,ITSUO NISHIOKA and AKIHIDE KODA Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . cinnacasol C20H30O7 ÏàËÆ¶È:70% Helvetica Chimica Acta 2009 92 2058-2062 Two New Diterpenes from the Twigs of Cinnamomum cassia Tran Minh Ngoc, Do Thi Ha, Ik-Soo Lee, Byung-Sun Min, Min-Kyun Na, Hyun-Ju Jung, Sang-Myung Lee, Ki-Hwan Bae Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . 4-oxo-5¦Á-androstan-17-one C18H28O2 ÏàËÆ¶È:60% Tetrahedron 1996 52 2325-2336 Shielding effect of ether C¤RO bond obtained from proton chemical shifts of 4-oxa-5¦Á- and 4-oxa-5¦Â-androstan-17-ones Yanyan Yang, Takeharu Haino, Shuji Usui, Yoshimasa Fukazawa Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . Boreovibrin F C19H30O5 ÏàËÆ¶È:60% Natural Products and Bioprospecting 2012 2 200-205 Twelve new compounds from the basidiomycete Boreostereum vibrans Jian-Hai DING, Tao FENG, Zheng-Hui LI, Liang LI, and Ji-Kai LIU Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . callicarpic acid A C20H30O2 ÏàËÆ¶È:55% Journal of Natural Products 2009 72 223-228 seco-Abietane Diterpenoids, a Phenylethanoid Derivative, and ntitubercular Constituents from Callicarpa pilosissima Jih-Jung Chen Hung-Ming Wu, Chien-Fang Peng,Ih-Sheng Chen, and Shih-Der Chu Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . vittatalactone C16H30O2 ÏàËÆ¶È:55% Journal of Natural Products 2005 68 26-30 Vittatalactone, a ¦Â-Lactone from the Striped Cucumber Beetle, Acalymma vittatum Bruce D. Morris, Rebecca R. Smyth, Stephen P. Foster, Michael P.Hoffmann, Wendell L. Roelofs, Stephan Franke, and Wittko Francke Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . pulchralide C C20H22O6Br4 ÏàËÆ¶È:55% Journal of Natural Products 2004 67 1295-1302 Chemical Investigation of Predator-Deterred Macroalgae from the Antarctic Peninsula Sridevi Ankisetty, Santhisree Nandiraju, Hla Win, Young Chul Park, Charles D. Amsler, James B. McClintock, Jill A. Baker, Thushara K. Diyabalanage, Albert Pasaribu, Maya P. Singh, William M. Maiese, Rosa D. Walsh, Michael J. Zaworotko, and Bill J. Baker Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . 3¦Â-acetoxy-17¦Á,16¦Á-(epoxymethano)-5¦Á-androstane C22H34O3 ÏàËÆ¶È:55% Steroids 2001 66 833-843 Configurational analysis and relative binding affinities of 16-methyl-5¦Á-androstane derivatives P¨¢l Tapolcs¨¢nyi, J¨¢nos Wölfling, Istv¨¢n T¨®th, Mih¨¢ly Sz¨¦csi, P¨¦ter Forg¨®, Gyula Schneider Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . 4¦Â-Acetoxy-9¦Â,10¦Â,15¦Á-trihydroxyprobotrydial C17H28O5 ÏàËÆ¶È:55% Phytochemistry 1995 38 647-650 Metabolites from a shake culture of Botrytis cinerea Isidro G. Collado, Rosario Hern¨¢ndez-Gal¨¢n, Rosa Dur¨¢n-Patr¨®n, Jes¨²s M. Cantoral Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . 14-acetoxy-T-cadinol ÏàËÆ¶È:55% Phytochemistry 1989 28 2717-2721 Sesquiterpenoids and phenolics of Pulicaria paludosa Arturo San Feliciano,Manuel Medarde,Marina Gordaliza,Esther Del Olmo,Jos¨¦ M. Miguel del Corral Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . O-acetylyamataimine C20H29NO6 ÏàËÆ¶È:55% Heterocycles 2003 60 1195-1198 New Pyrrolizidine Alkaloids from Ligularia tsangchanensis Aimin Tan, Zhengtao Wang,* Hongping He, Mian Zhang, and Xiaojiang Hao Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . manadic acid B methyl ester ÏàËÆ¶È:55% Tetrahedron 1995 51 12195-12202 Two Cytotoxic 3,6-Epidioxy Fatty Acids from an Indonesian Sponge, Plakortis sp. 1 Toshio Ichiba, Paul J Scheuer, Michelle Kelly-Borges Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . (1R,4R,4aS,7R,8aR)-7-hydroxy-4-isopropyl-1,6-dimethyl-1,2,3,4,4a,7,8,8a-octahydronaphthalen-1-yl acetate C17H28O2 ÏàËÆ¶È:55% Russian Journal of Organic Chemistry 2006 42 1321-1324 Inhibition of intramolecular reactions of (+)-¦Ä-cadinol O. Yu. Krasnoslobodtseva, F. A. Valeev, O. V. Shitikova and G. A. Tolstikov Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . 7,13-abietadien-3¦Â-ol ÏàËÆ¶È:55% Chinese Traditional and Herbal Drugs 2013 44 532-536 Diterpenoids from barks of Ceriops decandra WANG Hui, WU Jun Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . compound 5 C20H34O4 ÏàËÆ¶È:55% European Journal of Organic Chemistry 2005 2005 5077-5083 Antimalarial Polyketide Cycloperoxides from the Marine SpongePlakortis simplex Claudio Campagnuolo, Ernesto Fattorusso, Adriana Romano, Orazio Taglialatela-Scafati, Nicoletta Basilico, Silvia Parapini and Donatella Taramelli Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . compound 1 ÏàËÆ¶È:55% Organic Magnetic Resonance 1984 22 736-738 Carbon-13 nuclear magnetic resonance spectra of some heterocyclic D-homoandrostanes Deanna Marcano, Jeannette De M¨¦ndez, Ana C. Ortiz and Mirna Salinas Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . compound 4 ÏàËÆ¶È:55% Organic Magnetic Resonance 1984 22 736-738 Carbon-13 nuclear magnetic resonance spectra of some heterocyclic D-homoandrostanes Deanna Marcano, Jeannette De M¨¦ndez, Ana C. Ortiz and Mirna Salinas Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . (4S,5S,6¦Á,8S,9¦Á,10S,13R)-9,13-epoxy-14-labdene-6,19-diol 19-acetate ÏàËÆ¶È:54.5% Journal of Natural Products 2000 63 226-229 Grindelane Diterpenoids from Stevia subpubescens Luisa U. Rom¨¢n, Jairo I. Cambr¨®n, Rosa E. del R¨ªo, Juan D. Hern¨¢ndez, Carlos M. Cerda-Garc¨ªa-Rojas, and Pedro Joseph-Nathan Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . (-)-(1R,2S,7R,8S,3E,11E)-18-acetoxycembra-2,8-oxa-3,11,15(17)-trien-7-ol C22H34O4 ÏàËÆ¶È:54.5% Bioorganic & Medicinal Chemistry 2013 21 242-256 Synthesis of cembranoid analogues and evaluation of their potential as quorum sensing inhibitors Edisson Tello, Leonardo Castellanos, Carmenza Duque Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . 2¦Á,17¦Â-Dihydroxy-5¦Á-androstan-3-one 17-acetate C21H32O4 ÏàËÆ¶È:52.3% Steroids 2004 69 173-179 The oxidation of ¦¤2, ¦¤2,4 and ¦¤4,6 steroids with RuO4 Domenica Musumeci, Giovanni N. Roviello, Donato Sica Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . (13S,14S)-14-Acetoxy-6¦Â-methoxy-3¦Á,5-cyclo-13,14-seco-5¦Á-androstan-17-one C22H34O4 ÏàËÆ¶È:52.3% Steroids 2004 69 511-514 Reaction of (13S)-13-iodo-6¦Â-methoxy-3¦Á,5-cyclo-13,14-seco-5¦Á-androstane-14,17-dione with hydroxylamine and its application to the synthesis of new 13,14-seco steroids Vladimir A. Khripach, Vladimir N. Zhabinskii, Anna I. Kuchto, Galina P. Fando, Yuliya Y. Zhiburtovich, Alexander S. Lyakhov, Alla A. Govorova, Marinus B. Groen, Jaap van der Louw, Aede de Groot Structure 13C NMR ̼Æ×Ä£Äâͼ |

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